Sandoz Posted August 7, 2026

Technical Expert- Global MS&T Capability Hub

Telangana, India Full time
Manufacturing & CMC

Sandoz is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Description Summary

The Technical Expert – Global MS&T, based in the Capability Hub, provides specialized technical support and product stewardship for assigned Sandoz manufacturing sites and external suppliers (CMOs). The role ensures robust, compliant, and well-controlled manufacturing processes through hands-on support in process validation, technical investigations, product transfers, and preparation of technical documentation. The position serves as a key technical interface across internal sites, external partners, Development (SDC), and ESO to enable reliable product supply and technical compliance.

Job Description

Position Purpose:

The Technical Expert – Global MS&T, based in the Capability Hub, provides specialized technical support and product stewardship for assigned Sandoz manufacturing sites and external suppliers (CMOs). The role ensures robust, compliant, and well-controlled manufacturing processes through hands-on support in process validation, technical investigations, product transfers, and preparation of technical documentation. The position serves as a key technical interface across internal sites, external partners, Development (SDC), and ESO to enable reliable product supply and technical compliance.

Your key responsibilities:

Your responsibilities include, but   not   limited to:

Technical Support & Product Stewardship: Provide technical expertise to assigned Sandoz manufacturing sites in areas such as process design, equipment understanding, process performance assessment, and troubleshooting. Act as the technical steward for assigned products/sites to ensure processes remain validated, controlled, and capable. Support continued process verification (CPV), data review, and process improvement activities to enhance process robustness. Ensure assigned products remain in a validated and compliant state as per MS&T and regulatory expectations. Contribute to investigations and prepare OPV reports, PPQ documentation, regulatory responses, and scale‑up proposals.

Validation & Compliance: Support process validation and cleaning validation activities for assigned sites and products. Review and approve validation protocols and reports to ensure scientific robustness and regulatory compliance. Ensure the availability and accuracy of required technical documentation prior to major technical activities, including technical changes at Sandoz sites and CMOs. Provide technical assessments and recommendations for deviations, change controls, CAPAs, and customer complaints.

Technical Interface & External Supplier Support: Act as a key technical contact between Sandoz sites, CMOs, and Global MS&T for assigned products. Support manufacturing and packaging process evaluations, equipment/technology compatibility assessments, and technology selection as needed. Provide technical input during ESO-led due‑diligence assessments and supplier evaluations. Ensure timely and accurate preparation of documentation needed for risk assessments and supplier qualification activities.

Product Transfers: Serve as the technical focal point for product transfers involving legacy or new development products. Support transfers from Development to commercial sites, between internal sites, and between Sandoz and external suppliers. Collaborate with Development teams to align on process design expectations during early-stage development. Ensure preparation, review, and readiness of transfer-related documentation (BMR/BPR, process descriptions, control strategies, etc.).

Cross‑Functional Collaboration & Knowledge Management: Enable timely and effective knowledge transfer related to product and process understanding across internal and external stakeholders. Support development, standardization, and sharing of best practices, technical learnings, and process know‑how across MS&T functions.

Lifecycle Management: Support identification, assessment, and implementation of alternate suppliers for raw materials or components. Contribute to reformulation or process refinement work where applicable. Perform risk assessments related to product/process improvement and compliance.

Provide any additional technical support required to ensure business continuity, regulatory adherence, and operational readiness. This may include participation in tactical or strategic initiatives beyond the responsibilities listed above, as needed by the business. Complete all compliance activities in accordance with updated P&O or organizational requirements, adapting to evolving regulations, policies, and business needs.

Maintain adherence to internal governance processes and support continuous improvement by adopting new practices and standards as required for the effective functioning of the department and the organization.

What you’ll bring to the role:

Essential   Requirements :

Bachelors/Masters. in Pharmacy, Pharmaceutical Technology, Chemical Engineering /Chemistry or equivalent scientific degree.

Minimum 8 years of experience in pharmaceutical (chemical) manufacturing.

Experience in a global/matrix environment in the pharmaceutical industry. Comprehensive know how in pharmaceutical (chemical) technology, Project Management experience, Drug Development experience. Sound experience of data handling and applied statistics.

Strong technical and analytical problem‑solving capability.

Clear and effective communication with cross‑functional partners.

Ability to work efficiently within a global matrix environment.

Structured approach to documentation, compliance, and data analysis.

Proactive ownership of technical responsibilities within assigned scope. Ability to prioritize and manage multiple parallel activities. Strong decision‑making supported by scientific rationale.

Why Sandoz?

Sandoz is the global leader in Biosimilar and Generic medicines, a segment of the healthcare industry that delivers 80% of the world’s medicines at 30% of the cost, touching the lives of more than 1 billion people across 100+ countries! While we are proud of our achievements, we have an ambition to do more so that everyone can achieve the basic human   right   of good health.

With investments in new development capabilities, production sites, new acquisitions, and partnerships, we   have the opportunity to   shape the future of Sandoz and help even more people gain access to low-cost, high-quality medicines, sustainably.

Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills, experience an agile and collegiate environment with impactful careers, where diversity of thought is welcomed and where personal growth is supported!

Join us, help us make healthcare fairer and faster.

Commitment to Diversity & Inclusion: 

We are   committed to building an outstanding, inclusive work environment and diverse   teams   representative of the patients and communities we serve.

Skills Desired

Applied Statistics, Assembly Language, Change Control, Chemical Engineering, Continual Improvement Process, Cost Reduction, Data Analytics, Electronic Components, General Hse Knowledge  , Including Gdp, Knowledge Of Capa, Knowledge Of Gmp, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Manufacturing Technologies, Process and Cleaning Validation, Process Control, Process Simulation, Risk Management, Root Cause Analysis (RCA), Scientific Method, Six Sigma, Statistical Analysis, Technology Transfer

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Telangana, India
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 1793 comparable Manufacturing & CMC roles across 130 biopharma companies.

1793Comparable roles tracked
1703Currently active
130Companies hiring similar roles
47Countries represented

Salary context

527 of 1793 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Senior Scientist II – CMC Developmental Sciences · AbbVie $0/hr – $0/hr (≈ $0–$0/yr)
Highest disclosed · Technical Operator, Packaging - 2nd Shift · Mylan Technologies, Inc. $37,000/yr – $800,000/yr
Peer group range $0 – $418,500 (median $135,233)

Where these roles are based

Top locations among the 1793 comparable roles

United States895
India116
Germany101
France74
Singapore70
Ireland64

+ 41 more countries

Seniority mix

789 of 1793 peers have a known seniority level

Senior258
Manager203
Associate82
Principal82
Director62
Associate Director61
Senior Director25
Intern/Fellow/Postdoc11
Executive/VP5

Therapeutic area mix

6 of 1793 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease4
Oncology1
Rare Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Pfizer Healthcare India Private Limited Vizag, India Associate
Same function Same country
40%similar
Pfizer Healthcare India Private Limited Vizag, India Associate
Same function Same country
40%similar
Pfizer Healthcare India Private Limited Chennai, India Manager
Same function Same country
40%similar
Bristol-Myers Squibb Business Services India Private Limited Hyderabad, India Manager
Same function Same country
40%similar
GlaxoSmithKline Pharmaceuticals Limited Worli Mumbai, India Manager
Same function Same country
40%similar
Sanofi India Limited Verna, India
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Associate - MSAT-Analytical
Pfizer Healthcare India Private Limited · Vizag, India · Associate
Function Therapeutic area Seniority Country
40%
Senior Manager, Principal Statistician
Bristol-Myers Squibb Business Services India Private Limited · Hyderabad, India · Manager
Function Therapeutic area Seniority Country
40%
Director, Documentation, Knowledge Management, & Automation
Amgen Technology Pvt Ltd. · Hyderabad, India · Director
Function Therapeutic area Seniority Country
40%
Contract Development & Mfg Mgr
Amgen Technology Pvt Ltd. · Hyderabad, India · Seniority not listed
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.